Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5217036 | Tetrahedron | 2014 | 6 Pages |
Abstract
A series of fluorinated fullerene-fused 1,3-dioxolanes have been facilely and efficiently synthesized in the presence of easily available LiClO4·3H2O. The influences of the number of fluoro-substituents and their positions linked to the phenyl ring on the isolated yield of fullerene-fused 1,3-dioxolanes have been studied in detail. Based on reaction facts, a possible reaction mechanism for the formation of fluorinated fullerene-fused 1,3-dioxolanes has been proposed. Furthermore, detailed ultraviolet absorption spectra, fluorescence emission spectra, and cyclic voltammogram further explain the optical properties and electronic transmission capabilities of the products.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hao-Nan Cheng, Yuan-Hai Zou, Jian-Min Zhang, Shan-Shan He, Su-Bo Shen, Hong-Mei Deng,